[Federal Register Volume 88, Number 14 (Monday, January 23, 2023)]
[Notices]
[Pages 4020-4021]
From the Federal Register Online via the Government Publishing Office [www.gpo.gov]
[FR Doc No: 2023-01199]


-----------------------------------------------------------------------

DEPARTMENT OF JUSTICE

Drug Enforcement Administration

[Docket No. DEA-1129]


Bulk Manufacturer of Controlled Substances Application: Siegfried 
USA, LLC

AGENCY: Drug Enforcement Administration, Justice.

ACTION: Notice of application.

-----------------------------------------------------------------------

SUMMARY: Siegfried USA, LLC has applied to be registered as a bulk 
manufacturer of basic class(es) of controlled substance(s). Refer to 
SUPPLEMENTARY INFORMATION listed below for further drug information.

DATES: Registered bulk manufacturers of the affected basic class(es), 
and applicants therefore, may submit electronic comments on or 
objections to the issuance of the proposed registration on or before 
March 24, 2023. Such persons may also file a written request for a 
hearing on the application on or before March 24, 2023.

ADDRESSES: The Drug Enforcement Administration requires that all 
comments be submitted electronically through the Federal eRulemaking 
Portal, which provides the ability to type short comments directly into 
the comment field on the web page or attach a file for lengthier 
comments. Please go to https://www.regulations.gov and follow the 
online instructions at that site for submitting comments. Upon 
submission of your comment, you will receive a Comment Tracking Number. 
Please be aware that submitted comments are not instantaneously 
available for public view on https://www.regulations.gov. If you have 
received a Comment Tracking Number, your comment has been successfully 
submitted and there is no need to resubmit the same comment.

SUPPLEMENTARY INFORMATION: In accordance with 21 CFR 1301.33(a), this 
is notice that on November 8, 2022, Siegfried USA, LLC, 33 Industrial 
Park Road, Pennsville, New Jersey 08070-3244, applied to be registered 
as a bulk manufacturer of the following basic class(es) of controlled 
substance(s):

------------------------------------------------------------------------
                                            Drug
          Controlled substance              code          Schedule
------------------------------------------------------------------------
Gamma Hydroxybutyric Acid...............     2010  I
Noroxymorphone..........................     9145  I
Hydromorphinol..........................     9301  I
Amphetamine.............................     1100  II
Lisdexamfetamine........................     1205  II
Methylphenidate.........................     1724  II
Amobarbital.............................     2125  II
Pentobarbital...........................     2270  II
Secobarbital............................     2315  II
Codeine.................................     9050  II
Oxycodone...............................     9143  II

[[Page 4021]]

 
Hydromorphone...........................     9150  II
Hydrocodone.............................     9193  II
Methadone...............................     9250  II
Methadone intermediate..................     9254  II
Morphine................................     9300  II
Oripavine...............................     9330  II
Thebaine................................     9333  II
Opium tincture..........................     9630  II
Oxymorphone.............................     9652  II
Tapentadol..............................     9780  II
------------------------------------------------------------------------

    The company plans to bulk manufacture the listed controlled 
substances in bulk for sale to its customers. No other activities for 
these drug codes are authorized for this registration.

Matthew Strait,
Deputy Assistant Administrator.
[FR Doc. 2023-01199 Filed 1-20-23; 8:45 am]
BILLING CODE P